Variant #0000568858 (NC_000019.9:g.7696678C>T, NM_001171155.1:c.*236C>T (PET100))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.7696678C>T
DNA change (hg38) g.7631792C>T
Published as PCP2(NM_001271830.1):c.260G>A (p.(Arg87Gln))
ISCN -
DB-ID PET100_000006
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00271 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PET100 NM_001171155.1 -?/. - c.*236C>T r.(=) p.(=)
XAB2 NM_020196.2 -?/. - c.-2265G>A r.(?) p.(=)
PCP2 NM_174895.1 -?/. - c.308G>A r.(?) p.(Arg103Gln)


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